Aluminum-alloy clad material and production method therefor, and heat exchanger using said aluminum-alloy clad material and production method therefor

ABSTRACT

A highly corrosion resistant and highly formable aluminum-alloy clad material, a method for producing the same, a heat exchanger using the same and a method for producing the same are shown. The present aluminum-alloy clad material has an aluminum alloy core material, an intermediate layer material clad on one surface of the core material and a brazing filler metal clad on the surface of the intermediate layer material that is not on the core material side, wherein a crystal grain size of the intermediate layer material before brazing heating is 60 μm or more, and in a cross section of the core material in a rolling direction before brazing heating, when R1 (μm) represents the crystal grain size in a plate thickness direction, and R2 (μm) represents the crystal grain size in the rolling direction, R1/R2 is 0.30 or less.

TECHNICAL FIELD

The present invention relates to a highly corrosion resistant and highly formable aluminum-alloy clad material and a production method thereof and specifically relates to a highly corrosion resistant and highly formable aluminum-alloy clad material which is preferably used as a material constituting a path of a refrigerant or hot compressed air in a heat exchanger such as a radiator and to a production method thereof. The invention further relates to a heat exchanger using the highly corrosion resistant and highly formable aluminum-alloy clad material and in particular relates to a part forming a flow path of an automobile heat exchanger and the like.

BACKGROUND ART

Since aluminum alloys are light, have high thermal conductivity and can exhibit high corrosion resistance by appropriate treatment, aluminum alloys are used for automobile heat exchangers such as radiators, capacitors, evaporators, heaters or intercoolers. As a tube material of an automobile heat exchanger, a two-layer clad material having an Al—Mn-based aluminum alloy such as 3003 alloy as the core and a brazing filler metal of an Al—Si-based aluminum alloy or a sacrificial anode material of an Al—Zn-based aluminum alloy clad on a surface of the core or a three-layer clad material in which a brazing filler metal of an Al—Si-based aluminum alloy is further clad on the other surface of the core of such a two-layer clad material is used. A heat exchanger is generally produced by combining a tube material of such a clad material with a corrugated fin material and brazing the materials at a high temperature around 600° C.

The tube shape is more complex in new heat exchangers used for recent automobiles in order to further improve the performance. Accordingly, it is now required that the materials have higher formability. The formability of a tube material has been adjusted by H14 refining type achieved by process annealing during cold rolling or by H24 refining type achieved by finish annealing after cold rolling. However, it has become difficult to satisfy the recent demand for high formability by refining alone.

In addition, when a corrosive liquid exists on the inner or outer surface of the tube of a heat exchanger, a hole may be made in the tube by pitting corrosion or the strength of pressure resistance may deteriorate because uniform corrosion reduces the tube thickness, resulting in the bursting of the tube. As a result, there is risk of the leakage of the air, coolant or refrigerant circulating inside. Moreover, when it is necessary to join a tube and a fin or to join a tube with itself for example, it is required that a brazing filler metal is provided on the surfaces. When the material is exposed to a severe corrosive environment due to snow melting salt or the like and a tube and a fin should be joined, for example in the case of the outer surface of the tube of a condenser, it has been attempted to balance the corrosion resistance and the brazing property by cladding the outer surface of the tube material with a layer having sacrificial anode effect as an intermediate layer and further cladding the outer surface with a brazing filler metal. However, as the tube shape has become complex as already described above, the corrosive liquid sometimes concentrates at a particular part, and simple cladding of an intermediate layer as in the conventional techniques is sometimes insufficient for preventing the leakage.

Techniques for improving the formability and the corrosion resistance separately have been proposed. For example, techniques for improving the formability or the electric resistance welding property of a clad material are shown in PTLs 1 and 2. However, the PTLs do not describe any means for improving the corrosion resistance of the sacrificial anode material. On the other hand, a technique for improving the corrosion resistance of a clad material is shown in PTL 3. However, the PTL does not describe any means for improving the formability of the clad material.

Specifically, regarding the clad material described in PTL 1, the electric resistance welding property of the material is improved by adjusting the mean grain size of the core material in a cross section at right angles to the longitudinal direction to 30 μm or less. With respect to the sacrificial anode material, it is defined that the area percentage of Mg₂Si with a grain size of 0.2 μm or more is 0.5% or less, however, this is also means for improving the electric resistance welding property. Only the amounts of Zn and Mg are defined regarding the corrosion resistance of the sacrificial anode material, and a technique which would improve the corrosion resistance more than the conventional techniques is not described or suggested at all.

With respect to the clad material described in PTL 2, the electric resistance welding property of the material is improved by using a core material with a fibrous structure. Regarding the sacrificial anode material, it is defined that the hardness of the core material and the hardness of the sacrificial anode material are 50 Hv or more and that the ratio of hardness (sacrificial anode material/core material) is less than 1.0, however, this is means for securing the fatigue strength after braze heating. Only the amounts of Zn and Mn are defined regarding the corrosion resistance of the sacrificial anode material also in this document, and a technique which would improve the corrosion resistance more than the conventional techniques is not described or suggested at all.

On the other hand, regarding the clad material described in PTL 3, the corrosion resistance in an alkaline environment is improved by adjusting the grain size of the sacrificial anode material to 100 to 700 μm. However, only the components are defined regarding the core material, and the structure, the mechanical properties and the like thereof are not described. Also, PTL 3 does not describe or suggest the improvement of the formability at all.

Furthermore, the sacrificial anode materials described in the PTLs are all clad on the surface of a material, and it is not disclosed that the sacrificial anode materials are provided as intermediate layers between a core material and a brazing filler metal.

CITATION LIST Patent Literature

PTL 1: JP-A-H8-291354

PTL 2: JP-A-2010-255014

PTL 3: JP-A-H11-209837

SUMMARY OF INVENTION Technical Problem

The invention has been completed to solve the problems and aims to provide an aluminum-alloy clad material which has excellent formability when used for example as a tube material of a heat exchanger and excellent corrosion resistance after brazing heating due to the intermediate layer material and a production method thereof and to provide a heat exchanger using the aluminum-alloy clad material and a production method thereof. Such a highly corrosion resistant and formability aluminum-alloy clad material can be preferably used as a part forming a flow path of an automobile heat exchanger.

Solution to Problem

The present inventors have conducted intensive studies on the problems, and as a result, the inventors have found that the problems can be solved by using a clad material composed of a core material and an intermediate layer material which have specific alloy compositions and metal structures for the clad material and thus completed the invention.

That is, in claim 1, the first embodiment of the invention is an aluminum-alloy clad material having an aluminum alloy core material, an intermediate layer material clad on one surface of the core material and a brazing filler metal clad on a surface of the intermediate layer material that is not on the core material side,

wherein the core material comprises an aluminum alloy comprising 0.05 to 1.50 mass % Si, 0.05 to 2.00 mass % Fe, 0.5 to 2.0 mass % Mn and a balance of Al and unavoidable impurities, the intermediate layer material comprises an aluminum alloy comprises 0.5 to 8.0 mass % Zn, 0.05 to 1.50 mass % Si, 0.05 to 2.00 mass % Fe and a balance of Al and unavoidable impurities, and the brazing filler metal comprises an aluminum alloy comprises 2.5 to 13.0 mass % Si, 0.05 to 1.20 mass % Fe and a balance of Al and unavoidable impurities,

a crystal grain size of the intermediate layer material before brazing heating is 60 μm or more, and in a cross section of the core material in a rolling direction before brazing heating, R1/R2 is 0.30 or less, where R1 (μm) is the crystal grain size in a plate thickness direction, and R2 (μm) is the crystal grain size in the rolling direction.

In claim 2 of the invention, the core material comprises the aluminum alloy further comprising one or, two or more selected from 0.05 to 0.50 mass % Mg, 0.05 to 1.50 mass % Cu, 0.05 to 0.30 mass % Ti, 0.05 to 0.30 mass % Zr, 0.05 to 0.30 mass % Cr and 0.05 to 0.30 mass % V in claim 1.

In claim 3 of the invention, the intermediate layer material comprises the aluminum alloy further comprising one or, two or more selected from 0.05 to 2.00 mass % Ni, 0.05 to 2.00 mass % Mn, 0.05 to 0.30 mass % Ti, 0.05 to 0.30 mass % Zr, 0.05 to 0.30 mass % Cr and 0.05 to 0.30 mass % V in claim 1 or 2.

In claim 4 of the invention, the brazing filler metal comprises the aluminum alloy further comprising one or, two or more selected from 0.5 to 8.0 mass % Zn, 0.05 to 1.50 mass % Cu, 0.05 to 2.00 mass % Mn, 0.05 to 0.30 mass % Ti, 0.05 to 0.30 mass % Zr, 0.05 to 0.30 mass % Cr and 0.05 to 0.30 mass % V in any one of claims 1 to 3.

In claim 5 of the invention, the brazing filler metal comprises the aluminum alloy further comprising one or two selected from 0.001 to 0.050 mass % Na and 0.001 to 0.050 mass % Sr in any one of claims 1 to 4.

In claim 6 of the invention, a method for producing the aluminum-alloy clad material according to any one of claims 1 to 5, comprising: a step of casting the aluminum alloys for the core material, the intermediate layer material and the brazing filler metal, respectively, a hot rolling step of hot rolling the cast intermediate layer material ingot and the cast brazing filler metal ingot to predetermined thicknesses, respectively, a cladding step of cladding the intermediate layer material rolled to the predetermined thickness on one surface of the core material ingot, and cladding the brazing filler metal rolled to the predetermined thickness on the surface of the intermediate layer material that is not on the core material side and thus obtaining a clad material, a hot clad rolling step of hot rolling the clad material, a cold rolling step of cold rolling the hot-clad-rolled clad material, and one or more annealing steps of annealing the clad material either during or after the cold rolling step or both during and after the cold rolling step, wherein in the hot clad rolling step, the rolling start temperature is 400 to 520° C., and the number of rolling passes each with a rolling reduction of 30% or more is restricted to five or less while the temperature of the clad material is 200 to 400° C., and the clad material is held at 200 to 560° C. for 1 to 10 hours in the annealing steps.

In claim 7, the second embodiment of the invention is an aluminum-alloy clad material having an aluminum alloy core material, an intermediate layer material clad on one surface of the core material, a brazing filler metal clad on the surface of the intermediate layer material that is not on the core material side, and a brazing filler metal clad on the other surface of the core material,

wherein the core material comprises an aluminum alloy comprising 0.05 to 1.50 mass % Si, 0.05 to 2.00 mass % Fe, 0.5 to 2.0 mass % Mn and a balance of Al and unavoidable impurities, the intermediate layer material comprises an aluminum alloy comprising 0.5 to 8.0 mass % Zn, 0.05 to 1.50 mass % Si, 0.05 to 2.00 mass % Fe and a balance of Al and unavoidable impurities, and the brazing filler metal clad on the surface of the intermediate layer material that is not on the core material side and the brazing filler metal clad on the other surface of the core material comprise an aluminum alloy comprising 2.5 to 13.0 mass % Si, 0.05 to 1.20 mass % Fe and a balance of Al and unavoidable impurities,

a crystal grain size of the intermediate layer material before brazing heating is 60 μm or more, and in a cross section of the core material in a rolling direction before brazing heating, R1/R2 is 0.30 or less, wherein R1 (μm) is the crystal grain size in a plate thickness direction, and R2 (μm) is the crystal grain size in the rolling direction.

In claim 8 of the invention, the core material comprises the aluminum alloy further comprising one or, two or more selected from 0.05 to 0.50 mass % Mg, 0.05 to 1.50 mass % Cu, 0.05 to 0.30 mass % Ti, 0.05 to 0.30 mass % Zr, 0.05 to 0.30 mass % Cr and 0.05 to 0.30 mass % V in claim 7.

In claim 9 of the invention, the intermediate layer material comprises the aluminum alloy further comprising one or, two or more selected from 0.05 to 2.00 mass % Ni, 0.05 to 2.00 mass % Mn, 0.05 to 0.30 mass % Ti, 0.05 to 0.30 mass % Zr, 0.05 to 0.30 mass % Cr and 0.05 to 0.30 mass % V in claim 7 or 8.

In claim 10 of the invention, the brazing filler metal clad on the surface of the intermediate layer material that is not on the core material side and the brazing filler metal clad on the other surface of the core material comprise the aluminum alloy further comprising one or, two or more selected from 0.5 to 8.0 mass % Zn, 0.05 to 1.50 mass % Cu, 0.05 to 2.00 mass % Mn, 0.05 to 0.30 mass % Ti, 0.05 to 0.30 mass % Zr, 0.05 to 0.30 mass % Cr and 0.05 to 0.30 mass % V in any one of claims 7 to 9.

In claim 11 of the invention, the brazing filler metal clad on the surface of the intermediate layer material that is not on the core material side and the brazing filler metal clad on the other surface of the core material comprise the aluminum alloy further comprising one or two selected from 0.001 to 0.050 mass % Na and 0.001 to 0.050 mass % Sr in any one of claims 7 to 10.

In claim 12 of the invention, a method for producing the aluminum-alloy clad material according to any one of claims 7 to 11, comprising: a step of casting the aluminum alloys for the core material, the intermediate layer material, the brazing filler metal clad on the surface of the intermediate layer material that is not on the core material side and the brazing filler metal clad on the other surface of the core material, respectively, a hot rolling step of hot rolling the cast intermediate layer material ingot, the cast brazing filler metal ingot clad on the surface of the intermediate layer material that is not on the core material side and the cast brazing filler metal ingot clad on the other surface of the core material to predetermined thicknesses, respectively, a cladding step of cladding the intermediate layer material rolled to the predetermined thickness on one surface of the core material ingot, cladding the brazing filler metal rolled to the predetermined thickness on the surface of the intermediate layer material that is not on the core material side, and cladding the brazing filler metal rolled to the predetermined thickness on the other surface of the core material ingot and thus obtaining a clad material, a hot clad rolling step of hot rolling the clad material, a cold rolling step of cold rolling the hot-clad-rolled clad material, and one or more annealing steps of annealing the clad material either during or after the cold rolling step or both during and after the cold rolling step, wherein in the hot clad rolling step, the rolling start temperature is 400 to 520° C., and the number of rolling passes each with a rolling reduction of 30% or more is restricted to five or less while the temperature of the clad material is 200 to 400° C., and the clad material is held at 200 to 560° C. for 1 to 10 hours in the annealing steps.

In claim 13 of the invention, a heat exchanger using the aluminum-alloy clad material according to any one of claims 1 to 5 and 7 to 11, wherein the crystal grain size of the intermediate layer material after brazing heating is 100 μm or more.

In claim 14 of the invention, a method for producing the heat exchanger according to claim 13, wherein an aluminum alloy material is brazed in an inert gas atmosphere with flux.

The aluminum-alloy clad material according to the invention can be formed excellently even into a complex tube shape when the aluminum-alloy clad material is used as a tube material of a heat exchanger for example, and the aluminum-alloy clad material exhibits excellent corrosion resistance after braze heating due to the intermediate layer material. A heat exchanger of an automobile or the like is provided using such an aluminum-alloy clad material as a part forming a flow path or the like. The clad material also has excellent brazing properties such as erosion resistance and is preferably used as a tube material of an automobile heat exchanger further in view of the lightness and the excellent thermal conductivity.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1

A schematic figure illustrating a crystal grain surrounded by grain boundaries in a rolled surface of an intermediate layer material.

FIG. 2

A schematic figure illustrating a crystal grain size R1 in the thickness direction and a crystal grain size R2 in the rolling direction in a cross section of a core material along the rolling direction.

FIG. 3

A polarized light microscopic image of a cross section along the rolling direction where a core material having a fibrous structure was subjected to anodic oxidation.

DESCRIPTION OF EMBODIMENTS

Preferable embodiments of the aluminum-alloy clad material exhibiting high corrosion resistance and high formability according to the invention, the production method thereof, the heat exchanger using the aluminum-alloy clad material and the production method thereof are explained in detail.

1. Layers Constituting Aluminum-Alloy Clad Material

The aluminum-alloy clad material according to the invention has excellent formability because the components and the metal structure of the core material are controlled properly, and the aluminum-alloy clad material has excellent corrosion resistance because the components and the metal structure of the intermediate layer material, which is clad on a surface of the core material, are controlled properly. Regarding the aluminum-alloy clad material according to the first embodiment of the invention, cladding on the other surface of the core material is not particularly restricted. For example, when the tube is produced by a process such as welding and it is not necessary to braze the tube and a fin, the other surface of the core material may be without cladding in the aluminum-alloy clad material according to the first embodiment of the invention. On the other hand, when the tube material is joined to itself by brazing or when the tube and a fin are brazed, the other surface of the core material is also clad with the brazing filler metal in the aluminum-alloy clad material according to the second embodiment of the invention.

The components of the core material, the intermediate layer material and the two brazing filler metals, namely the brazing filler metal which is clad on the surface of the intermediate layer material that is not on the core material side (referred to as “a first brazing filler metal” below) and the brazing filler metal which is clad on the other surface of the core material (referred to as “a second brazing filler metal” below) are explained below.

2. Core Material

An aluminum alloy comprising 0.05 to 1.50 mass % (simply indicated by “%” below) Si, 0.05 to 2.00% Fe and 0.5 to 2.0% Mn as essential elements and a balance of Al and unavoidable impurities is used for the core material in the first embodiment and the second embodiment.

An aluminum alloy which further comprises one or, two or more selected from 0.05 to 0.50% Mg, 0.05 to 1.50% Cu, 0.05 to 0.30% Ti, 0.05 to 0.30% Zr, 0.05 to 0.30% Cr and 0.05 to 0.30% V as optional additional elements in addition to the essential elements may be used for the core material in the both of above embodiments.

Furthermore, besides the essential elements and the optional additional elements, unavoidable impurities may be comprised each in an amount of 0.05% or less and in a total amount of 0.15% for the core material in the both of above embodiments.

As the aluminum alloy used for the core material of the both of above embodiments, Al—Mn-based alloys such as JIS 3000 series alloys including JIS 3003 alloy and the like for example are preferably used. While each component is explained below, each of said ingredients is common to the first and second embodiments.

Si:

Si forms an Al—Fe—Mn—Si-based intermetallic compound with Fe and Mn and improves the strength of the core material through dispersion strengthening or improves the strength of the core material through solid solution strengthening by diffusing into the aluminum parent phase to form a solid solution. The Si content is 0.05 to 1.50%. For a content less than 0.05%, use of high purity aluminum metal is required, resulting in high cost. On the other hand, when the content exceeds 1.50%, the melting point of the core material decreases, and the core material is more likely to melt during brazing. A preferable Si content is 0.10 to 1.20%.

Fe:

Fe forms an Al—Fe—Mn—Si-based intermetallic compound with Si and Mn and improves the strength of the core material through dispersion strengthening. The Fe content is 0.05 to 2.00%. For a content less than 0.05%, use of high purity aluminum metal is required, resulting in high cost. On the other hand, when the content exceeds 2.00%, a giant intermetallic compound tends to be formed during casting, and the plasticity deteriorates. A preferable Fe content is 0.10 to 1.50%.

Mn:

Mn forms an Al—Mn—Si-based or Al—Fe—Mn—Si-based intermetallic compound with Si and improves the strength of the core material through dispersion strengthening or improves the strength of the core material through solid solution strengthening by diffusing into the aluminum parent phase to form a solid solution. The Mn content is 0.5 to 2.0%. When the content is less than 0.5%, the effects are insufficient, while when the content exceeds 2.0%, a giant intermetallic compound tends to be formed during casting, and the plasticity deteriorates. A preferable Mn content is 0.8 to 1.8%.

Mg:

Mg may be comprised because precipitation of Mg₂Si improves the strength of the core material. The Mg content is 0.05 to 0.50%. When the content is less than 0.05%, the effect is insufficient, while when the content exceeds 0.50%, a brazing becomes difficult. A preferable Mg content is 0.10 to 0.40%.

Cu:

Cu may be comprised because Cu improves the strength of the core material through solid solution strengthening. The Cu content is 0.05 to 1.50%. When the content is less than 0.05%, the effect is insufficient, while when the content exceeds 1.50%, the aluminum alloy is more likely to crack during casting. A preferable Cu content is 0.30 to 1.00%.

Ti:

Ti may be comprised because Ti improves the strength of the core material through solid solution strengthening. The Ti content is 0.05 to 0.30%. When the content is less than 0.05%, the effect is insufficient. When the content exceeds 0.30%, a giant intermetallic compound tends to be formed, and the plasticity deteriorates. A preferable Ti content is 0.10 to 0.20%.

Zr:

Zr may be comprised because Zr has effects of improving the strength of the core material through solid solution strengthening and coarsening the crystal grains after braze heating by precipitation of an Al—Zr-based intermetallic compound. The Zr content is 0.05 to 0.30%. When the content is less than 0.05%, the effects cannot be obtained. On the other hand, when the content exceeds 0.30%, a giant intermetallic compound tends to be formed, and the plasticity deteriorates. A preferable Zr content is 0.10 to 0.20%.

Cr:

Cr may be comprised because Cr has effects of improving the strength of the core material through solid solution strengthening and coarsening the crystal grains after braze heating by precipitation of an Al—Cr-based intermetallic compound. The Cr content is 0.05 to 0.30%. When the content is less than 0.05%, the effects cannot be obtained. On the other hand, when the content exceeds 0.30%, a giant intermetallic compound tends to be formed, and the plasticity deteriorates. A preferable Cr content is 0.10 to 0.20%.

V:

V may be comprised because V improves the strength of the core material through solid solution strengthening and also improves the corrosion resistance. The V content is 0.05 to 0.30%. When the content is less than 0.05%, the effects cannot be obtained. On the other hand, when the content exceeds 0.30%, a giant intermetallic compound tends to be formed, and the plasticity deteriorates. A preferable V content is 0.10 to 0.20%.

At least one of the elements Mg, Cu, Ti, Zr, Cr and V may be added to the core material when needed.

3. Intermediate Layer Material

An aluminum alloy containing 0.5 to 8.0% Zn, 0.05 to 1.50% Si and 0.05 to 2.00% Fe as essential elements and a balance of Al and unavoidable impurities is used for the intermediate layer material in the first and second embodiments.

An aluminum alloy which further contains one or, two or more selected from 0.05 to 2.00% Ni, 0.05 to 2.00% Mn, 0.05 to 0.30% Ti, 0.05 to 0.30% Zr, 0.05 to 0.30% Cr and 0.05 to 0.30% V as optional additional elements may be used for the intermediate layer material in the both of embodiments above in addition to the essential elements. Furthermore, besides the essential elements and the optional additional elements, unavoidable impurities may be contained each in an amount of 0.05% or less and in a total amount of 0.15% in the both of embodiments above. While each component is explained below, each of said ingredients is common to the first and second embodiments.

Zn:

Zn can shift the pitting potential in the less noble direction and can improve the corrosion resistance through sacrificial anticorrosion effect by generating a potential difference from the core material. The Zn content is 0.5 to 8.0%. When the content is less than 0.5%, the effect of improving the corrosion resistance through the sacrificial anticorrosion effect cannot be obtained sufficiently. On the other hand, when the content exceeds 8.0%, the corrosion rate increases, and the intermediate layer material is lost at an early stage, resulting in the deterioration of the corrosion resistance. A preferable Zn content is 1.0 to 6.0%.

Si:

Si forms an Al—Fe—Si based intermetallic compound with Fe and forms an Al—Fe—Mn—Si based intermetallic compound with Fe and Mn when Mn is comprised at the same time. Si thus improves the strength of the intermediate layer material through dispersion strengthening or improves the strength of the intermediate layer material through solid solution strengthening by diffusing into the aluminum parent phase to forma solid solution. Moreover, since Si shifts the potential of the intermediate layer material in the more noble direction, Si inhibits the sacrificial anticorrosion effect and deteriorates the corrosion resistance. The Si content is 0.05 to 1.50%. For a content less than 0.05%, use of high purity aluminum metal is required, resulting in high cost. On the other hand, when the content exceeds 1.50%, the pitting potential of the intermediate layer material is shifted in the more noble direction, and the sacrificial anticorrosion effect is lost, resulting in the deterioration of the corrosion resistance. A preferable Si content is 0.10 to 1.20%.

Fe:

Fe forms an Al—Fe—Si-based intermetallic compound with Si and forms an Al—Fe—Mn—Si-based intermetallic compound with Si and Mn when Mn is contained at the same time. Fe thus improves the strength of the intermediate layer material through dispersion strengthening. The amount of Fe is 0.05 to 2.00%. For a content less than 0.05%, use of high purity aluminum metal is required, resulting in high cost. On the other hand, when the content exceeds 2.00%, a giant intermetallic compound tends to be formed during casting, and the plasticity deteriorates. A preferable Fe content is 0.10 to 1.50% or less.

Ni:

Ni forms an Al—Ni-based intermetallic compound or an Al—Fe—Ni-based intermetallic compound with Fe. The intermetallic compounds have significantly noble corrosion potential as compared to the aluminum matrix and thus act as cathode sites of corrosion. Accordingly, when the intermetallic compounds are dispersed in the intermediate layer material, the sites for the onset of corrosion are dispersed. As a result, the corrosion in the depth direction is unlikely to progress, resulting in the improvement of the corrosion resistance, thus Ni may be comprised. Further, Ni has an effect to improve the strength of the intermediate layer material. So, the Ni content is 0.05 to 2.00% to improve the corrosion resistance and the strength. When the content is less than 0.05%, the effects to improve the corrosion resistance and strength cannot be obtained sufficiently. On the other hand, when the content exceeds 2.00%, a giant intermetallic compound tends to be formed during casting, and the plasticity deteriorates. A preferable Ni content is 0.10 to 1.50%.

Mn:

Mn may be comprised because Mn improves the strength and the corrosion resistance of the intermediate layer material. The Mn content is 0.05 to 2.00%. When the content exceeds 2.00%, a giant intermetallic compound tends to be formed during casting, and the plasticity deteriorates. On the other hand, when the content is less than 0.05%, the effects cannot be obtained sufficiently. A preferable Mn content is 0.05 to 1.80%.

Ti:

Ti may be comprised because Ti improves the strength of the intermediate layer material through solid solution strengthening and also improves the corrosion resistance. The Ti content is 0.05 to 0.30%. When the content is less than 0.05%, the effects cannot be obtained. When the content exceeds 0.30%, a giant intermetallic compound tends to be formed, and the plasticity deteriorates. A preferable Ti content is 0.05 to 0.20%.

Zr:

Zr may be comprised because Zr has effects of improving the strength of the intermediate layer material through solid solution strengthening and coarsening the crystal grains after braze heating by precipitation of an Al—Zr-based intermetallic compound. The Zr content is 0.05 to 0.30%. When the content is less than 0.05%, the effects cannot be obtained. On the other hand, when the content exceeds 0.30%, a giant intermetallic compound tends to be formed, and the plasticity deteriorates. A preferable Zr content is 0.10 to 0.20%.

Cr

Cr may be comprised because Cr has effects of improving the strength of the intermediate layer material through solid solution strengthening and coarsening the crystal grains after braze heating by precipitation of an Al—Cr-based intermetallic compound. The Cr content is 0.05 to 0.30%. When the content is less than 0.05%, the effects cannot be obtained. When the content exceeds 0.30%, a giant intermetallic compound tends to be formed, and the plasticity deteriorates. A preferable Cr content is 0.10 to 0.20%.

V:

V may be comprised because V improves the strength of the intermediate layer material through solid solution strengthening and also improves the corrosion resistance. The V content is 0.05 to 0.30%. When the content is less than 0.05%, the effects cannot be obtained. When the content exceeds 0.30%, a giant intermetallic compound tends to be formed, and the plasticity deteriorates. A preferable V content is 0.05 to 0.20%.

At least one of the elements Ni, Mn, Ti, Zr, Cr and V may be added to the intermediate layer material when needed.

4. Brazing Filler Metal

For the first and second brazing filler metals in the first and second embodiments, an aluminum alloy containing 2.5 to 13.0% Si and 0.05 to 1.20% Fe as essential elements and a balance of Al and unavoidable impurities is used.

The brazing filler metals for the both of the embodiments above in addition to the essential elements may contain one or, two or more selected from 0.5 to 8.0% Zn, 0.05 to 1.50% Cu, 0.05 to 2.00% Mn, 0.05 to 0.30% Ti, 0.05 to 0.30% Zr, 0.05 to 0.30% Cr and 0.05 to 0.30% V as the first optional element. Moreover, one or two selected from 0.001 to 0.050 mass % Na and 0.001 to 0.050 mass % Sr may be contained as a second optional additional elements in addition to the essential elements or to the essential elements and the first optional additional elements, Furthermore, besides the essential elements and the first and/or the second optional additional elements, unavoidable impurities may be contained each in an amount of 0.05% or less and in a total amount of 0.15%. While each component is explained below, each of said ingredients is common to the first and second embodiments.

Si:

The containing of Si decreases the melting point of the brazing filler metal and generates a liquid phase, and thus brazing becomes possible. The Si content is 2.5 to 13.0%. When the content is less than 2.5%, only a small amount of liquid phase is generated, and brazing is unlikely to function. On the other hand, when the content exceeds 13.0%, the amount of Si which diffuses into the material to be brazed such as a fin becomes excessive in the case where the brazing filler metal is used for a tube material for example, and the material to be brazed melts. A preferable Si content is 3.5 to 12.0%.

Fe:

Since Fe tends to form an Al—Fe-based or Al—Fe—Si-based intermetallic compound, Fe decreases the effective Si amount for brazing and deteriorates the brazing property. The Fe content is 0.05 to 1.20%. For a content less than 0.05%, use of high purity aluminum metal is required, resulting in high cost. On the other hand, when the content exceeds 1.20%, the effective Si amount for brazing decreases, and brazing becomes insufficient. A preferable Fe content is 0.10 to 0.50%.

Zn:

Zn may be comprised because Zn can shift the pitting potential in the less noble direction and can improve the corrosion resistance through sacrificial anticorrosion effect by generating a potential difference from the core material. The Zn content is 0.5 to 8.0%. When the content is less than 0.5%, the effect of improving the corrosion resistance through the sacrificial anticorrosion effect cannot be obtained sufficiently. On the other hand, when the content exceeds 8.0%, the corrosion rate increases, and the sacrificial anticorrosion layer is lost at an early stage, resulting in the deterioration of the corrosion resistance. A preferable Zn content is 1.0 to 6.0%.

Cu:

Cu may be comprised because Cu improves the strength of the brazing filler metal through solid solution strengthening. The Cu content is 0.05 to 1.50%. When the content is less than 0.05%, the effect is insufficient, while when the content exceeds 1.50%, the aluminum alloy is more likely to crack during casting. A preferable Cu content is 0.30 to 1.00%. When the brazing filler metal contains Zn, a preferable Cu content is 0.05 to 0.60%. Since Cu shifts the pitting potential in the more noble direction, it is possible for the sacrificial anticorrosion effect due to Zn to be lost when Cu content exceeds 0.6%.

Mn:

Mn may be comprised because Mn improves the strength of the brazing filler metal and the corrosion resistance. The Mn content is 0.05 to 2.00%. When the content exceeds 2.00%, a giant intermetallic compound tends to be formed during casting, and the plasticity deteriorates. On the other hand, when the content is less than 0.05%, the effects cannot be obtained sufficiently. A preferable Mn content is 0.05 to 1.80%.

Ti:

Ti may be comprised because Ti improves the strength of the brazing filler metal through solid solution strengthening and also improves the corrosion resistance. The Ti content is 0.05 to 0.30%. When the content is less than 0.05%, the effects cannot be obtained. When the content exceeds 0.30%, a giant intermetallic compound tends to be formed, and the plasticity deteriorates. A preferable Ti content is 0.10 to 0.20%.

Zr:

Zr may be comprised because Zr has effects of improving the strength of the brazing filler metal through solid solution strengthening and coarsening the crystal grains after braze heating by precipitation of an Al—Zr-based intermetallic compound. The Zr content is 0.05 to 0.30%. When the content is less than 0.05%, the effects cannot be obtained. When the content exceeds 0.30%, a giant intermetallic compound tends to be formed, and the plasticity deteriorates. A preferable Zr content is 0.10 to 0.20%.

Cr:

Cr may be comprised because Cr has effects of improving the strength of the brazing filler metal through solid solution strengthening and coarsening the crystal grains after braze heating by precipitation of an Al—Cr-based intermetallic compound. The Cr content is 0.05 to 0.30%. When the content is less than 0.05%, the effects cannot be obtained. When the content exceeds 0.30%, a giant intermetallic compound tends to be formed, and the plasticity deteriorates. A preferable Cr content is 0.10 to 0.20%.

V:

V may be comprised because V improves the strength of the brazing filler metal through solid solution strengthening and also improves the corrosion resistance. The V content is 0.05 to 0.30%. When the content is less than 0.05%, the effects cannot be obtained. When the content exceeds 0.30%, a giant intermetallic compound tends to be formed, and the plasticity deteriorates. A preferable V content is 0.10 to 0.20%.

Na and Sr:

Na and Sr exhibit an effect of making the Si grains in the brazing filler metal fine. The Na and Sr contents are 0.001 to 0.050%. When the contents are less than 0.001%, the effect cannot be obtained sufficiently. On the other hand, when the contents exceed 0.050%, the oxide layer becomes thick, and the brazing property deteriorates. The contents are preferably 0.003 to 0.020%.

At least one of the elements Zn, Cu, Mn, Ti, Zr, Cr, V, Na and Sr may be added to the brazing filler metal when needed.

5. Crystal Grain Size of Intermediate Layer Material

In the aluminum-alloy clad material of the invention, the crystal grain size of the intermediate layer material before brazing heating is prescribed to 60 μm or more and the crystal grain size of the intermediate layer material after brazing heating is prescribed to 100 μm or more. This aims at improving the corrosion resistance of the intermediate layer material after brazing heating. As shown in FIG. 1, the crystal grain size here means the equivalent circle diameter of a crystal grain, where the crystal grain is an area surrounded by grain boundaries when the rolled surface of the intermediate layer material is observed. A grain boundary is a boundary with a difference between the neighboring crystal orientations of 20 degrees or more. The method for measuring the crystal grain size is not particularly restricted, but electron backscatter diffraction (EBSD) is generally used. The reasons for the restriction are explained below.

The intermediate layer material is clad for the purpose of sacrificial anticorrosion in which corrosion perforation of a tube is prevented by the corrosion being made to spread on the plane. When the corrosion rate of the intermediate layer material is high, however, the intermediate layer material is lost at an early stage, and the sacrificial anticorrosion effect is lost, leading to corrosion perforation of the tube.

As a result of intensive studies, the inventors have found that the corrosion rate at the crystal grain boundaries in the intermediate layer material is higher than that in the crystal grains and that the corrosion rate can be restricted by decreasing the area of the crystal grain boundaries. To decrease the area of the crystal grain boundaries means to increase the crystal grain size. Upon investigation in further detail, it has been found that the corrosion rate of the intermediate layer material is restricted and the aluminum-alloy clad material has excellent corrosion resistance when the crystal grain size of the intermediate layer material is 100 μm or more after brazing heating. When the crystal grain size of the intermediate layer material is less than 100 μm after brazing heating, the corrosion rate of the intermediate layer material is high, and the sacrificial anticorrosion effect is lost at an early stage. Thus, effective corrosion resistance cannot be obtained. The crystal grain size of the intermediate layer material after brazing heating is preferably 120 μm or more. The upper limit of the crystal grain size of the intermediate layer material after brazing heating is not particularly restricted, but a value of 1000 μm or more is difficult to achieve.

The inventors have further investigated and found a positive correlation between the grain size of the intermediate layer material before brazing heating and the crystal grain size of the intermediate layer material after brazing heating. That is, in order to obtain an intermediate layer material with a large crystal grain size after brazing heating, it is necessary that the crystal grain size of the intermediate layer material before brazing heating is large. As a result of further investigation into this point, it has been found that the crystal grain size of the intermediate layer material after brazing heating becomes 100 μm or more when the crystal grain size of the intermediate layer material before brazing heating is 60 μm or more. When the crystal grain size of the intermediate layer material before brazing heating is less than 60 μm, the crystal grain size of the intermediate layer material after brazing heating becomes less than 100 μm. In this regard, the crystal grain size before brazing heating is preferably 80 μm or more. The upper limit of the crystal grain size of the intermediate layer material before brazing heating is not particularly restricted, but a value of 1000 μm or more is difficult to achieve.

6. Crystal Grain Size of Core Material

With respect to the aluminum-alloy clad material of the invention, in a cross section of the core material in a rolling direction before brazing heating, when R1 (μm) represents the crystal grain size in a plate thickness direction, and R2 (μm) represents the crystal grain size in the rolling direction, R1/R2 is restricted to 0.30 or less. The ratio is an index to improve the formability of the clad material before brazing heating. As shown in FIG. 2, the crystal grain sizes R1 and R2 (μm) here are defined as the maximum diameter of a crystal grain in the plate thickness direction and the maximum diameter in the rolling direction, respectively, where the crystal grain is an area surrounded by crystal grain boundaries when a cross section along the rolling direction of the clad material is observed. A grain boundary is a boundary with a difference between the neighboring crystal orientations of 20 degrees or more. The method for measuring the crystal grain sizes is not particularly restricted, but electron backscatter diffraction (EBSD) is generally used. In this regard, in the case where the degree of processing of the core material is very high, a fibrous structure like the structure shown in FIG. 3 is observed when the core material is subjected to anodic oxidation after mirror polishing and the surface subjected to the anodic oxidation is observed using a polarized light microscope. In such a case, the crystal grains are completely crushed flat in the thickness direction, and this case is defined as R1=0.

As already described above, so far, the formability of an aluminum alloy has been improved by adjusting the mechanical properties by the refining type determined by the conditions of process annealing or the reduction in a subsequent step. However, when a step such as bending under severe conditions is conducted, the material cracks. The inventors have conducted intensive studies and as a result found that excellent formability can be obtained when the crystal grains of the core material before brazing heating are flat in the rolling direction in a cross section along the rolling direction. In the invention, the ratio R1/R2 is used as an index of the flatness of the crystal grains. Upon investigation in detail by the inventors, it has been found that the crystal grains of the core material are flat enough and excellent formability is exhibited when the ratio R1/R2 is 0.30 or less. When the ratio R1/R2 exceeds 0.30, the flatness of the crystal grains of the core material is insufficient, and excellent formability cannot be achieved. The ratio R1/R2 is preferably 0.20 or less. The ratio R1/R2 is preferably small, because the degree of flatness becomes higher and the processability becomes better. As described above, the ratio R1/R2 may be 0 with R1=0.

7. Production Method of Aluminum-Alloy Clad Material 7-1. Embodiments of Production Method

The method for producing the aluminum-alloy clad material of the first embodiment according to the invention includes a step of casting the aluminum alloys for the core material, the intermediate layer material and the first brazing filler metal, respectively, a hot rolling step of hot rolling the cast intermediate layer material ingot and the cast first brazing filler metal to predetermined thicknesses, respectively, a cladding step of cladding the intermediate layer material rolled to the predetermined thickness on one surface of the core material ingot, cladding the first brazing filler metal rolled to the predetermined thickness on the other surface of the core material ingot and thus obtaining a clad material, a hot clad rolling step of hot rolling the clad material, a cold rolling step of cold rolling the hot-clad-rolled clad material, and one or more annealing steps of annealing the clad material either during or after the cold rolling step or both during and after the cold rolling step.

The method for producing the aluminum-alloy clad material of the second embodiment according to the invention includes a step of casting the aluminum alloys for the core material, the intermediate layer material, the first brazing filler metal and the second brazing filler metal, respectively, a hot rolling step of hot rolling the cast intermediate layer material ingot, the cast first brazing filler metal ingot and the cast second brazing filler metal ingot to predetermined thicknesses, respectively, a cladding step of cladding the intermediate layer material rolled to the predetermined thickness on one surface of the core material ingot, cladding the brazing first filler metal rolled to the predetermined thickness on the surface of the intermediate layer material that is not on the core material side and cladding the brazing second filler metal rolled to the predetermined thickness on the other surface of the core material ingot and thus obtaining a clad material, a hot clad rolling step of hot rolling the clad material, a cold rolling step of cold rolling the hot-clad-rolled clad material, and one or more annealing steps of annealing the clad material either during or after the cold rolling step or both during and after the cold rolling step.

7-2. Casting Step and Hot Rolling Step

The conditions of the step of casting the core material, the first and second brazing filler metals and the intermediate layer material are not particularly restricted, but in general, water-cooled semi-continuous casting is employed. In the step of hot rolling the core material, the intermediate layer material and the first and second brazing filler metals to the predetermined thicknesses, the heating conditions are preferably a temperature of 400 to 560° C. and a period of 1 to 10 hours. When the temperature is lower than 400° C., the plasticity is poor, and edge cracking or the like may be caused during rolling. In the case of a high temperature exceeding 560° C., the ingots may melt during heating. When the heating time is shorter than one hour, since the temperatures of the ingots become uneven, the plasticity is poor, and edge cracking or the like may be caused during rolling. When the heating time exceeds 10 hours, the productivity deteriorates notably.

7-3. Hot Clad Rolling Step

During the methods for producing the aluminum-alloy clad materials of the first and second embodiments, in the hot clad rolling step, the rolling start temperature is 400 to 520° C., and the number of rolling passes each with a rolling reduction of 30% or more is restricted to five or less while the temperature of the clad material is 200 to 400° C. The hot clad rolling step may be divided into a rough rolling step and a finish rolling step. In the finish rolling step, a reversing or tandem rolling mill is used. In a reversing rolling mill, a pass is defined as a one-way rolling, and in a tandem rolling mill, a pass is defined as rolling with a set of rolls.

First, the rolling pass is explained. As already described above, in the aluminum-alloy clad material of the invention, it is necessary to increase the crystal grain size of the intermediate layer material before brazing heating. The crystal grains of the intermediate layer material are formed in an annealing step during the production, and as the strain accumulated in the intermediate layer material before annealing becomes greater, the driving force for the grain growth generated during annealing becomes larger, and larger crystal grains can be obtained. On the other hand, in the aluminum-alloy clad material of the invention, it is necessary that the crystal grains of the core material are flat before brazing heating. The crystal grains of the core material are also formed in an annealing step during the production. As the strain accumulated in the core material before annealing becomes smaller, the driving force for the grain growth in the plate thickness direction generated during annealing becomes smaller, and as a result, flat crystal grains can be obtained.

That is, to increase the size of the crystal grains of the intermediate layer material and to flatten the crystal grains of the core material are incompatible. Accordingly, it has been difficult with the conventional techniques to achieve both. However, as a result of intensive studies, the inventors have found that both can be achieved by controlling the hot clad rolling step.

When a rolling pass with a large rolling reduction is conducted while the temperature of the hot clad rolling is relatively low, larger shear strain tends to be caused also in the center of the material. More specifically, in the hot clad rolling step, when the number of rolling passes with a rolling reduction of 30% or more is restricted to five or less while the temperature of the clad material is 200 to 400° C., the shear strain caused in the core material becomes small, and the crystal grains of the core material before braze heating can be made flat. While the temperature of the clad material is higher than 400° C. in the hot clad rolling step, dynamic recovery occurs during the hot clad rolling, and the shear strain caused in the core material does not become large even by a rolling pass with a rolling reduction of 30% or more. Thus, the flatness of the crystal grains of the core material is not affected. On the other hand, when the temperature of the clad material is lower than 200° C. in the hot clad rolling step, cracking occurs during the hot rolling, and a clad material cannot be produced. Also, when the rolling reduction is less than 30% per pass, the shear strain caused in the core material does not become large, and the flatness of the crystal grains of the core material is not affected. The number of rolling passes with a rolling reduction of 30% or more is preferably four or less while the temperature of the clad material is 200 to 400° C. The rolling reduction is preferably 35% or more. When a rolling pass with a rolling reduction exceeding 50% is applied, cracking of the material or the like may occur.

On the other hand, even when the number of rolling passes with a rolling reduction of 30% or more is restricted to five or less while the temperature of the clad material is 200 to 400° C. in the hot clad rolling step, large shear strain is caused in the intermediate layer material, which is close to the surface layer of the clad material. Thus, grains grow sufficiently in the intermediate layer material during process annealing, and large crystal grains can be formed in the intermediate layer material. That is, by the control in the hot clad rolling, the crystal grains of the intermediate layer material can be coarsened and the crystal grains of the core material can be made flat.

Next, the rolling start temperature is explained. The grain size of the intermediate layer material before brazing heating is controlled by adjusting the rolling start temperature in the hot clad rolling step. When the start temperature of the hot clad rolling is 520° C. or lower, large shear strain is caused in the intermediate layer material during the hot clad rolling, and the crystal grain size of the intermediate layer material before brazing heating can be increased. When the start temperature of the hot clad rolling exceeds 520° C., dynamic recovery occurs in the intermediate layer material during the hot clad rolling, and the shear strain becomes smaller. Thus, the crystal grain size of the intermediate layer material before brazing heating cannot be increased. On the other hand, when the material temperature is lower than 400° C. at the start of the hot clad rolling, the material cracks during rolling. Thus, the start temperature of the hot clad rolling is 400 to 520° C. The start temperature of the hot clad rolling is preferably 420 to 500° C. or lower.

In the hot clad rolling step, the lower limit is not particularly set for the number of the passes with a rolling reduction of 30% or more conducted while the temperature of the clad material is 200 to 400° C. However, when no pass with a rolling reduction of 30% or more is included, many passes with a rolling reduction less than 30% are required to obtain the desired effects, and the productivity deteriorates. Accordingly, it is preferable that one or more passes with a rolling reduction of 30% or more are included. Moreover, the clad material is preferably heated at 400 to 560° C. for 1 to 10 hours before the hot clad rolling. When the heating temperature is lower than 400° C., the material temperature during rolling becomes too low, and thus the material may crack during rolling. On the other hand, when the heating temperature exceeds 560° C., the brazing filler metal may melt. When the heating time is shorter than one hour, the material temperature is unlikely to become even. On the other hand, when the heating time exceeds 10 hours, the productivity may deteriorate notably. The thickness after the hot clad rolling is not particularly restricted, but in general, a thickness of around 2.0 to 5.0 mm is preferable.

7-4. Annealing Step

In the methods for producing the aluminum-alloy clad materials of the first and second embodiments, one or more annealing steps of annealing the clad material either during or after the cold rolling step or both during and after the cold rolling step are conducted. Specifically, (1) one or more process annealing steps are conducted during the cold rolling step; (2) one final annealing step is conducted after the cold rolling step; or (3) (1) and (2) are conducted. In the annealing steps, the clad material is held at 200 to 560° C. for 1 to 10 hours.

The annealing steps are conducted for the purpose of adjusting the strain of the material, and by the steps, the intermediate layer material can be recrystallized, and large crystal grains as those described above can be obtained. When the temperature of the clad material is lower than 200° C. in the annealing steps or when the holding time is shorter than one hour, the recrystallization of the intermediate layer material is not completed. When the annealing temperature exceeds 560° C., the brazing filler metal may melt. Even when the holding time exceeds 10 hours, there is no problem with the properties of the clad material, but the productivity deteriorates notably.

The upper limit of the number of the annealing steps is not particularly restricted, but the number is preferably three or less in order to avoid the increase of costs due to the increased number of steps.

7-5. Homogenization Step

The ingot obtained by casting the aluminum alloy core material may be subjected to a homogenization step before the cladding step. In the homogenization step, the ingot is preferably held at 450 to 620° C. for 1 to 20 hours. When the temperature is lower than 450° C. or when the holding time is shorter than one hour, the homogenization effect may be insufficient, while the core material ingot may melt when the temperature exceeds 620° C. Also, when the holding time exceeds 20 hours, the homogenization effect is saturated, and the step is an uneconomic step.

7-6. Cladding Rate

In the aluminum-alloy clad material of the invention, the cladding rate of the intermediate layer material (one surface) is preferably 3 to 25%. As described above, during the hot clad rolling step in the production steps, it is necessary that large shear strain is caused only in the intermediate layer material. However, when the cladding rate of the intermediate layer material exceeds 25%, sufficient shear strain cannot be caused in the entire intermediate layer material, and in some cases, the intermediate layer material cannot entirely be recrystallized. On the other hand, when the cladding rate of the intermediate layer material is less than 3%, the intermediate layer material is too thin, and thus the intermediate layer material cannot always be clad on the entire surface of the core material in the hot clad rolling. The cladding rate of the intermediate layer material is more preferably 5 to 20%.

The cladding rates of the first and second brazing filler metals are not particularly restricted, but these brazing filler metals are generally clad with cladding rates of around 3 to 30%.

8. Heat Exchanger

The aluminum-alloy clad material is preferably used as a part of a heat exchanger such as a tube material and a header plate and in particular as a tube material. For example, a tube material in which a medium such as a coolant flows is produced by bending the aluminum-alloy clad material and brazing the overlapped edges. Also, a header plate having a hole which is joined with an end of a tube material is produced by processing the aluminum-alloy clad material. The heat exchanger according to the invention has a structure obtained for example by combining the tube material, a fin material and the header plate and brazing the materials at once.

As described above, a heat exchanger produced by brazing using the materials of the invention under general conditions is characterized in that the crystal grain size of the intermediate layer material of the aluminum-alloy clad material after braze heating is 100 μm or more. The characteristic can improve the corrosion resistance of the intermediate layer material after brazing heating as described above.

The heat exchanger is assembled by attaching header plates to both ends of a tube material and placing a fin material on the outer surface of the tube material. Next, the overlapped edges of the tube material, the fin material and the outer surface of the tube material, the ends of the tube material and the header plates are each joined by one braze heating at once. While a Nocolok brazing method, a vacuum brazing method and a fluxless brazing method are used as the brazing method, the Nocolok brazing method is preferable. Brazing is generally conducted by heating at a temperature of 590 to 610° C. for 2 to 10 minutes, preferably by heating at a temperature of 590 to 610° C. for two to six minutes. The brazed materials are generally cooled at a cooling rate of 20 to 500° C./rain.

EXAMPLES

Next, the invention is explained in further detail based on Examples of the invention and Comparative Examples, but the invention is not restricted by the Examples.

Core material alloys with the alloy compositions shown In Table 1, intermediate layer material alloys with the alloy compositions shown in Table 2 and brazing filler metal alloys with the alloy compositions shown in Table 3 were each cast by DC casting and finished by facing both surfaces. The thicknesses of the ingots after facing were all 400 mm. With respect to the brazing filler metals and the intermediate layer materials, the cladding rates which would give the desired thicknesses as the final thicknesses were calculated, and the materials were subjected to a heating step at 520° C. for three hours and then hot rolled to the predetermined thicknesses which were the necessary thicknesses when the materials were combined. Furthermore, homogenization conditions of the core material are shown in Table 4.

TABLE 1 Alloy Alloy Composition (mass %) Symbol Si Fe Cu Mn Mg Ti Zr Cr V Al Example of A1 0.50 0.20 — 1.1 — — — — — Balance Invention A2 0.50 0.20 — 1.1 0.50 0.05 — — — Balance A3 0.50 0.20 — 1.5 0.05 — 0.05 — — Balance A4 0.05 2.00 — 1.1 — — — 0.05 — Balance A5 1.50 0.05 0.05 0.5 — — — — 0.05 Balance A6 0.50 0.20 — 2.0 — 0.30 0.30 0.30 0.30 Balance A7 1.20 0.20 0.05 1.1 — — — — — Balance A8 0.50 0.20 1.50 1.1 — — — — — Balance Comparative A9 1.60 0.20 — 1.1 — — — — — Balance Example A10 0.50 0.20 — 1.1 0.60 — 0.15 — — Balance A11 0.50 2.20 — 1.5 — 0.15 0.15 — — Balance A12 0.50 0.20 — 1.5 — 0.40 0.40 0.40 0.40 Balance A13 0.50 0.20 — 2.2 — — — — — Balance A14 0.50 0.20 1.60 1.1 — — — — — Balance A15 0.50 0.20 — 0.4 — 0.05 0.05 — — Balance

TABLE 2 Alloy Alloy Composition (mass %) Symbol Zn Si Fe Mn Mg Ni Ti Zr Cr V Al Example of B1 2.0 0.20 0.20 — — — — — — Balance Invention B2 0.5 0.05 0.05 — — — 0.05 — — — Balance B3 8.0 0.20 0.20 — — — 0.30 0.30 0.30 0.30 Balance B4 2.0 1.50 0.20 — — — — 0.05 — — Balance B5 2.0 0.20 2.00 — — — — — 0.05 — Balance B6 2.0 0.20 0.20 0.05 — — — — — 0.05 Balance B7 2.0 0.20 0.20 2.00 — — — — — — Balance B8 2.0 0.20 0.20 — — 0.05 — — — — Balance B9 2.0 0.20 0.20 — — 2.00 — — — — Balance Comparative B10 2.0 1.60 0.20 — — — — — — — Balance Example B11 2.0 0.20 2.20 — — — — — — — Balance B12 2.0 0.20 0.20 — — — 0.40 0.40 0.40 0.40 Balance B13 0.4 0.20 0.20 — — — — — — — Balance B14 9.0 0.20 0.20 — — — — — — — Balance B15 2.0 0.20 0.20 — — 2.20 — — — — Balance B16 2.0 0.20 0.20 2.20 — — — — — — Balance

TABLE 3 Alloy Alloy Composition (mass %) Symbol Si Fe Cu Mn Zn Ti Zr Cr V Na Sr Al Example of C1 10.0 0.20 — — — — — — — — — Balance Invention C2 2.5 0.20 — — — 0.05 — — — 0.001 — Balance C3 13.0 0.20 — — — — 0.05 — — — 0.001 Balance C4 10.0 0.05 — — — — — 0.05 — 0.050 — Balance C5 10.0 1.20 — — — — — — 0.05 — 0.050 Balance C6 10.0 0.20 0.05 — — 0.30 0.30 0.30 0.30 — — Balance C7 10.0 0.20 1.50 — — — — — — — — Balance C8 10.0 0.20 — 0.05 — — — — — — — Balance C9 10.0 0.20 — 2.00 — — — — — — — Balance C10 10.0 0.20 — — 0.5 — — — — — — Balance C11 10.0 0.20 — — 8.0 — — — — — — Balance C12 10.0 0.20 0.60 — 0.5 — — — — — — Balance Comparative C13 2.0 0.20 — — — — — — — — — Balance Example C14 14.0 0.20 — — — — — — — — — Balance C15 10.0 1.40 — — — — — — — — — Balance C16 10.0 0.20 1.60 — — — — — — — — Balance C17 10.0 0.20 — 2.20 — — — — — — — Balance C18 10.0 0.20 — — — 0.40 0.40 0.40 0.40 — — Balance C19 10.0 0.20 — — — — — — — 0.060 — Balance C20 10.0 0.20 — — — — — — — — 0.060 Balance C21 10.0 0.20 — — 0.4 — — — — — — Balance C22 10.0 0.20 — — 9.0 — — — — — — Balance C23 10.0 0.20 0.70 — 0.5 — — — — — — Balance

Using the alloys, an intermediate layer material in Table 2 was provided on a surface of a core material alloy, and a brazing filler metal in Table 3 was provided on the surface of the intermediate layer material that was not on the core material side. In some of the examples, a brazing filler metal in Table 3 was provided also on the other surface of the core material. Here, the brazing filler metal which was clad on the surface of the intermediate layer that was not on the core material side is referred to as the first brazing filler metal, and the brazing filler metal which was clad on the other surface of the core material is referred to as the second brazing filler metal. The cladding rates of the first and second brazing filler metals and the intermediate layer material were all 10%.

Such combined materials were subjected to a heating step and then to a hot clad rolling step, and three-layer and four-layer clad materials each with a thickness of 3.5 mm were produced. The temperatures and the times of the heating step and the start temperatures and the finish temperatures of the hot clad rolling step are shown in Table 4. Furthermore, in the hot clad rolling step, the clad materials were subjected to one or more rolling passes each with a rolling reduction of 30% or more while the temperatures of the clad materials were 200° C. to 400° C., and the numbers of the rolling passes are shown in Table 4. Because the start temperatures were all 400° C. or higher and the finish temperatures were all 200° C. or higher and lower than 400° C. in the Examples of the invention, it is obvious that there was a pass (passes) while the temperatures of the clad materials were 200° C. to 400° C. After the hot clad rolling step, the clad materials were subjected to cold rolling. Some of the clad materials were subjected to batch process annealing (once or twice) during the cold rolling and then to final cold rolling, and clad material samples each with a final thickness of 0.3 mm were produced. Some of the other clad materials were subjected once to the final annealing after the final cold rolling step without the process annealing, and clad material samples each with a final thickness of 0.3 mm were produced. Further some of the other clad materials were subjected to both of the process annealing and final annealing, and clad material samples each with a final thickness of 0.3 mm were produced. The reductions of the cold rolling after the process annealing were all 30%. The conditions of the process annealing are shown in Table 4. As shown in Table 4, neither process annealing nor final annealing was conducted in E14 to 16. The hot clad rolling was not conducted in E16. The conditions of homogenization of the core materials are shown in Table 4.

TABLE 4 Homogenization Step Hot Clad Rolling Step of Core Material Heating Step Start Finish Process Annealing Final Annealing Temper- Temper- Temper- Temper- Temper- Temper- ature Time ature Time ature ature Number of Time ature Time ature (° C.) (h) (° C.) (h) (° C.) (° C.) Passes *1) (h) (° C.) Number (h) (° C.) Example of E1 — — 480 5 460 230 3 5 350 1 — — Invention E2 — — 400 5 400 200 2 — — — 5 350 E3 — — 550 5 520 250 4 — — — 1 350 E4 — — 480 1 430 210 3 — — — 10  350 E5 — — 480 10 460 220 3 5 200 1 5 200 E6 — — 480 5 460 230 3 5 560 1 5 200 E7 — — 480 5 460 230 5 5 350 2 — — E8 450  1 480 5 460 230 3 5 350 1 — — E9 620 10 480 5 460 230 3 5 350 1 — — Comparative E10 — — 480 5 460 250 6 — — — 5 350 Example E11 — — 560 5 520 250 6 — — — 5 350 E12 — — 560 5 530 250 3 — — — 5 350 E13 — — 480 5 460 230 3 — — — 5 180 E14 — — 480 5 460 230 3 — — — 5 570 E15 — — 480 5 460 230 3   0.5 350 2 — — E16 — — 380 5 330 150 3 — — — — — E17 — — 480 0.5 350 170 3 — — — — — E18 — — 570 5 — — — — — — — — *1) the number of rolling passes each with a rolling reduction of 30% or more while the temperatureof the clad material is 200 to 400° C.

The manufactureability was given a mark “0” when no problem arose during the production steps and the material could be rolled to the final thickness of 0.3 mm. The manufacturability was given a mark “x” when the material cracked during the casting or the rolling and thus the material could not be rolled to the final thickness of 0.3 mm or when a clad material could not be produced due to melting during the heating step before the hot clad rolling step or during the process annealing step or due to poor pressure bonding during the hot clad rolling. The results are shown in Tables 5 to 7. The combinations of the core material alloy, the intermediate layer material alloy and the brazing filler metal alloy and of the respective clad materials are also shown in Tables 5 to 7.

TABLE 5 Alloy Brazing Property First Second First Second Tensile Strength after Brazing Brazing Brazing Brazing Brazing Heating Core Intermediate Filler Filler Manufac- Filler Filler Form- Determi- No. Material Layer Material Metal Metal Step turability Metal Metal ability (MPa) nation Example of 1 A1 B1 C1 C1 E1 ◯ ◯ ◯ ◯ 142 ◯ Invention 2 A2 B2 C2 C10 E1 ◯ ◯ ◯ ◯ 179 ◯ 3 A3 B3 C3 C11 E1 ◯ ◯ ◯ ◯ 148 ◯ 4 A4 B4 C4 C12 E1 ◯ ◯ ◯ ◯ 142 ◯ 5 A5 B5 C5 — E1 ◯ ◯ — ◯ 160 ◯ 6 A6 B6 C6 — E1 ◯ ◯ — ◯ 149 ◯ 7 A7 B7 C7 — E1 ◯ ◯ — ◯ 159 ◯ 8 A8 B8 C8 — E1 ◯ ◯ — ◯ 188 ◯ 9 A1 B9 C9 — E1 ◯ ◯ — ◯ 140 ◯ 10 A1 B1 C10 — E1 ◯ ◯ — ◯ 145 ◯ 11 A1 B1 C11 — E1 ◯ ◯ — ◯ 142 ◯ 12 A1 B1 C12 — E1 ◯ ◯ — ◯ 143 ◯ Crystal Grain size before Crystal Grain size after Corrosion Resistance Brazing Heating Brazing Heating First Second Intermediate Core Material Intermediate Brazing Brazing Layer Material R1 R2 Layer Material Filler Filler No. (μm) (μm) (μm) R1/R2 (μm) Metal Metal Example of 1 105 14 152 0.09 175 ⊚ — Invention 2 110 25 120 0.21 183 ⊚ ◯ 3 130 20 135 0.15 217 ⊚ ◯ 4 145 27 124 0.22 242 ⊚ ◯ 5 140 13 185 0.07 233 ⊚ — 6 155 10 196 0.05 258 ⊚ — 7 164 10 204 0.05 273 ⊚ — 8 98 11 113 0.10 163 ⊚ — 9 85 17 150 0.11 142 ⊚ — 10 101 21 162 0.13 168 ⊚ — 11 111 14 171 0.08 185 ⊚ — 12 120 23 115 0.20 200 ⊚ —

TABLE 6 Alloy Brazing Property First Second First Second Brazing Brazing Brazing Brazing Core Intermediate Filler Filler Manufac- Filler Filler No. Material Layer Material Metal Metal Step turability Metal Metal Comparative 13 A9 B1 C1 — E1 ◯ X — Example 14 A10 B1 C1 — E1 ◯ X — 15 A11 B1 C1 — E1 X — — 16 A12 B1 C1 — E1 X — — 17 A13 B1 C1 — E1 X — — 18 A14 B1 C1 — E1 X — — 19 A15 B1 C1 — E1 ◯ ◯ — 20 A1 B10 C1 — E1 ◯ X — 21 A1 B11 C1 — E1 X — — 22 A1 B12 C1 — E1 X — — 23 A1 B13 C1 — E1 ◯ ◯ — 24 A1 B14 C1 — E1 ◯ ◯ — 25 A1 B15 C1 — E1 X — — 26 A1 B16 C1 — E1 X — — 27 A1 B1 C13 — E1 ◯ X — 28 A1 B1 C14 — E1 ◯ X — 29 A1 B1 C15 — E1 ◯ X — 30 A1 B1 C16 — E1 X — — 31 A1 B1 C17 — E1 X — — 32 A1 B1 C18 — E1 X — — 33 A1 B1 C19 — E1 ◯ X — 34 A1 B1 C20 — E1 ◯ X — 35 A1 B1 C1 C21 E1 ◯ ◯ ◯ 36 A1 B1 C1 C22 E1 ◯ ◯ ◯ 37 A1 B1 C1 C23 E1 ◯ ◯ ◯ Grain size before Tensile Strength after Brazing Heating Brazing Heating Intermediate Core Material Form- Determi- Layer Material R1 R2 No. ability (MPa) nation (μm) (μm) (μm) R1/R2 Comparative 13 ◯ 167 ◯ 100  6 214 0.03 Example 14 ◯ 186 ◯ 109 23  96 0.24 15 — — — — — — — 16 — — — — — — — 17 — — — — — — — 18 — — — — — — — 19 ◯ 113 X 102 20 102 0.20 20 ◯ 146 ◯ 183 16 161 0.10 21 — — — — — — — 22 — — — — — — — 23 ◯ 145 ◯ 102 19 170 0.11 24 ◯ 144 ◯  96 17 166 0.10 25 — — — — — — — 26 — — — — — — — 27 ◯ 142 ◯ 118 14 154 0.09 28 ◯ 144 ◯ 103 17 169 0.10 29 ◯ 142 ◯ 121 16 158 0.10 30 — — — — — — — 31 — — — — — — — 32 — — — — — — — 33 ◯ 145 ◯ 108 16 137 0.12 34 ◯ 141 ◯ 100 15 134 0.11 35 ◯ 143 ◯ 104 15 149 0.10 36 ◯ 140 ◯ 109 15 154 0.10 37 ◯ 140 ◯ 115 13 159 0.08 Crystal Grain size after Corrosion Resistance Brazing Heating First Second Intermediate Brazing Brazing Layer Material Filler Filler No. (μm) Metal Metal Comparative 13 167 — — Example 14 182 — — 15 — — — 16 — — — 17 — — — 18 — — — 19 170 ⊚ — 20 305 — — 21 — — — 22 — — — 23 170 X — 24 160 X — 25 — — — 26 — — — 27 197 — — 28 172 — — 29 202 — — 30 — — — 31 — — — 32 — — — 33 180 ⊚ — 34 167 ⊚ — 35 173 ⊚ X 36 182 ⊚ X 37 192 ⊚ X

TABLE 7 Alloy Brazing Property First Second First Second Tensile Strength after Brazing Brazing Brazing Brazing Brazing Heating Core Intermediate Filler Filler Manufac- Filler Filler Form- Determi- No. Material Layer Material Metal Metal Step turability Metal Metal ability (MPa) nation Example of 38 A1 B1 C1 — E2 ◯ ◯ — ◯ 148 ◯ Invention 39 A1 B1 C1 — E3 ◯ ◯ — ◯ 139 ◯ 40 A1 B1 C1 — E4 ◯ ◯ — ◯ 140 ◯ 41 A1 B1 C1 — E5 ◯ ◯ — ◯ 143 ◯ 42 A1 B1 C1 — E6 ◯ ◯ — ◯ 144 ◯ 43 A1 B1 C1 — E7 ◯ ◯ — ◯ 141 ◯ 44 A1 B1 C1 — E8 ◯ ◯ — ◯ 139 ◯ 45 A1 B1 C1 — E9 ◯ ◯ — ◯ 136 ◯ Comparative 46 A1 B1 C1 — E10 ◯ ◯ — X 142 ◯ Example 47 A1 B1 C1 — E11 ◯ ◯ — X 139 ◯ 48 A1 B1 C1 — E12 ◯ ◯ — ◯ 136 ◯ 49 A1 B1 C1 — E13 ◯ ◯ — ◯ 142 ◯ 50 A1 B1 C1 — E14 X — — — — — 51 A1 B1 C1 — E15 ◯ ◯ — ◯ 140 ◯ 52 A1 B1 C1 — E16 X — — — — — 53 A1 B1 C1 — E17 X — — — — — 54 A1 B1 C1 — E18 X — — — — — Crystal Grain size beforing Crystal Grain size after Corrosion Resistance Brazing Heating Brazing Heating First Second Intermediate Core Material Intermediate Brazing Brazing Layer Material R1 R2 Layer Material Filler Filler No. (μm) (μm) (μm) R1/R2 (μm) Metal Metal Example of 38 132  7 181 0.04 220 ⊚ — Invention 39 62 20 131 0.15 103 ⊚ — 40 112 13 157 0.08 187 ⊚ — 41 97 23 142 0.16 162 ⊚ — 42 132 18 150 0.12 220 ⊚ — 43 110 43 155 0.28 183 ⊚ — 44 110 17 152 0.11 183 ⊚ — 45 103 20 152 0.13 172 ⊚ — Comparative 46 130 38 96 0.40 217 ⊚ — Example 47 131 35 99 0.35 218 ⊚ — 48 56 23 151 0.15 93 X — 49 Fibrous 15 152 0.10 82 X — 50 — — — — — — — 51 Fibrous 18 167 0.11 75 X — 52 — — — — — — — 53 — — — — — — — 54 — — — — — — —

The following items of the clad material samples were evaluated, and the results are also shown in Tables 5 to 7. In this regard, in the examples with the manufacturability marked with “x” in Tables 6 and 7, samples could not be produced, and thus the following evaluation could not be conducted.

(Evaluation of Formability)

JIS5 test pieces were cut out of the respective clad material samples, stretched by 5% in the direction parallel to the rolling direction and bent at 180° with a bending radius R of 0.05 mm with the intermediate layer material surface inside. A resin was applied to the bent R cross sections so that the cross sections could be observed, and the cross sections were subjected to mirror polishing. Then, the test pieces were evaluated as to whether there was a crack using an optical microscope. As a result, the formability was determined to be at an acceptable level (◯) when there was no crack in the core material and at an unacceptable level (x) when there was a crack in the core material. The occurrence of cracks in the intermediate layer materials, the brazing filler metals and the intermediate layer materials was not evaluated.

(Evaluation of Brazing Property)

A fin material with a thickness of 0.07 mm, refining type of H14 and an alloy composition of 3003 alloy containing 1.0% Zn was prepared and corrugated, and thus a heat exchanger fin material was prepared. The fin material was placed on the first brazing filler metal side or the second brazing filler metal side of a clad material sample, and the sample was dipped in an aqueous 5% fluoride flux solution and subjected to braze heating at 600° C. for three minutes by the Nocolok brazing method, thereby producing a miniature core sample. After the brazing, the fin was removed, and the fin joint ratio was determined from the ratio of the number of the contacts between the fin and the brazing filler metal (the number of the ridges) and the parts where the fillets were formed. The brazing property was determined to be at an acceptable level (◯) when the fin joint ratio of the miniature core sample was 95% or more and the clad material sample and the fin did not melt. On the other hand, the brazing property was determined to be at an unacceptable level (x) when the following cases (1) and (2) applied or the case (1) or (2) applied: (1) the fin joint ratio was less than 95%; and (2) at least one of the clad material sample and the fin melted.

(Measurement of Tensile Strength after Brazing Heating)

The clad material samples were subjected to heat treatment at 600° C. for three minutes (corresponding to braze heating) and then to a tensile test under the conditions of a speed of tensile testing of 10 mm/min and a gauge length of 50 mm according to JIS 22241. The tensile strengths were read from the obtained stress-strain curves. As a result, the tensile strength was determined to be at an acceptable level (◯) when the value was 120 MPa or more and at an unacceptable level (x) when the value was less than 120 MPa.

(Measurement of Crystal Grain Size of Intermediate Layer Material)

The surfaces of clad material samples before brazing heating (at 600° C. for three minutes treatment corresponding to brazing heating) and clad material samples after brazing heating were polished and a brazing filler metal was removed therefrom. Subsequently, L-LT surface of the intermediate layer material is subjected to mirror polishing, and samples for the measurement of the intermediate layer material crystal grain size were thus prepared. An area of 2 mm×2 mm of each sample was analyzed by EBSD of a SEM (scanning electron microscope). Boundaries with a difference between crystal orientations of 20 degrees or more were detected as the grain boundaries from the results, and the crystal grain sizes (equivalent circle diameters) were calculated. Ten random points were selected for the measurement, and the arithmetic mean was regarded as the crystal grain size. When the recrystallization of the intermediate layer material had not been completed, the intermediate layer material had a fibrous structure, and the crystal grain size could not be measured. Such samples are indicated by “fibrous”.

(Measurement of Grain Size of Core Material)

Clad material samples before brazing heating (at 600° C. for three minutes treatment corresponding to brazing heating) and clad material samples after brazing heating were used. A resin was applied to the clad material samples and mirror polishing was conducted in such a manner that the cross sections along the rolling directions became the surfaces to be measured. Thus, samples for the measurement of the core material crystal grains were prepared. An area with a length of 2 mm and a thickness of 0.2 mm of each sample was analyzed by EBSD of a SEM, and from the results, boundaries with a difference between crystal orientations of 20 degrees or more were detected as the grain boundaries to detect the crystal grains. The maximum diameter R1 of a crystal grain in the thickness direction and the maximum diameter R2 in the rolling direction were measured, and the value R1/R2 was calculated. Ten random crystal grains in a single field were measured, and the arithmetic mean was regarded as the ratio R1/R2. When no crystal grain boundary was detected by EBSD, the mirror-polished samples were subjected to anodic oxidation and observed using a polarized light microscope. The R1 was regarded as zero when a fibrous structure like the structure shown in FIG. 3 was observed.

(Corrosion Resistance)

The same miniature core samples as those used for evaluating the brazing property were used. The surfaces which were not joined with the fins were masked with an insulating resin, and the surfaces which were joined with the fins were subjected to a CASS test as a test surface based on JIS-H8502 for 500 hours and 1000 hours. As a result, the CASS corrosion resistance was determined to be excellent and at an acceptable level (⊚) when corrosion perforation did not develop in the clad material within the 1000 hours, at an acceptable level (◯) when corrosion perforation did not develop in the clad material within the 500 hours and at an unacceptable level (x) when corrosion perforation developed within the 500 hours. In this regard, all the first brazing filler metals were evaluated, and the second brazing filler metals were evaluated only when the second brazing filler metals contained Zn. Regarding the samples which were not clad with any second brazing filler metal, the surfaces of the core materials which were not the surfaces clad with the first brazing filler metals (the surfaces with the exposed core materials) were not evaluated. Appropriate miniature core samples could not be produced when the brazing property was “x”, and thus the samples were excluded from the evaluation.

Examples 1 to 12 and 38 to 45 of the invention satisfied the conditions defined in the invention, and the manufacturability, the formability, the brazing properties, the tensile strengths after brazing and the corrosion resistance were all at acceptable levels.

On the contrary, in Comparative Example 13, since the Si content of the core material was too much, the brazing property of the first brazing filler metal was unacceptable.

In Comparative Example 14, since the Mg content of the core material was too much, the brazing property of the first brazing filler metal was unacceptable.

In Comparative Example 15, since the Fe content of the core material was too much, a crack was caused during the rolling, and a brazing sheet could not be produced. Thus, the manufacturability was unacceptable.

In Comparative Example 16, since the Ti, Zr, Cr and V contents of the core material were too much, a crack was caused during the rolling, and a brazing sheet could not be produced. Thus, the manufacturability was unacceptable.

In Comparative Example 17, since the Mn content of the core material was too much, a crack was caused during the rolling, and a brazing sheet could not be produced. Thus, the manufacturability was unacceptable.

In Comparative Example 18, since the Cu content of the core material was too much, a crack was caused during the casting, and a brazing sheet could not be produced. Thus, the manufacturability was unacceptable.

In Comparative Example 19, since the Mn content of the core material was too little, the tensile strength after the brazing heating was unacceptable.

In Comparative Example 20, since the Si content of the intermediate layer material was too much, the brazing property of the first brazing filler metal was unacceptable.

In Comparative Example 21, since the Fe content of the intermediate layer material was too much, a crack was caused during the rolling, and a brazing sheet could not be produced. Thus, the manufacturability was unacceptable.

In Comparative Example 22, since the Ti, Zr, Cr and V contents of the intermediate layer material were too much, a crack was caused during the rolling, and a brazing sheet could not be produced. Thus, the manufacturability was unacceptable.

In Comparative Example 23, since the Zn content of the intermediate layer material was too little, the corrosion resistance of the first brazing filler metal side was unacceptable.

In Comparative Example 24, since the Zn content of the intermediate layer material was too much, the corrosion resistance of the first brazing filler metal was unacceptable.

In Comparative Example 25, since the Ni content of the intermediate layer material was too much, a crack was caused during the rolling, and a brazing sheet could not be produced. Thus, the manufacturability was unacceptable.

In Comparative Example 26, since the Mn content of the intermediate layer material was too much, a crack was caused during the rolling, and a brazing sheet could not be produced. Thus, the manufacturability was unacceptable.

In Comparative Example 27, since the Si content of the first brazing filler metal was too little, the brazing property of the first brazing filler metal was unacceptable.

In Comparative Example 28, since the Si content of the first brazing filler metal was too much, the brazing property of the first brazing filler metal was unacceptable.

In Comparative Example 29, since the Fe content of the first brazing filler metal was too much, the brazing property of the first brazing filler metal was unacceptable.

In Comparative Example 30, since the Cu content of the first brazing filler metal was too much, a crack was caused during the rolling, and a brazing sheet could not be produced. Thus, the manufacturability was unacceptable.

In Comparative Example 31, since the Mn content of the first brazing filler metal was too much, a crack was caused during the rolling, and a brazing sheet could not be produced. Thus, the manufacturability was unacceptable.

In Comparative Example 32, since the Ti, Zr, Cr and V contents of the first brazing filler metal was too much, a crack was caused during the rolling, and a brazing sheet could not be produced. Thus, the manufacturability was unacceptable.

In Comparative Example 33, since the Na content of the brazing filler metal was too much, the brazing property of the first brazing filler metal was unacceptable.

In Comparative Example 34, since the Sr content of the brazing filler metal was too much, the brazing property of the first brazing filler metal was unacceptable.

In Comparative Example 35, since the Zn content of the brazing filler metal was too little, the corrosion resistance of the second brazing filler metal was unacceptable.

In Comparative Example 36, since the Zn content of the brazing filler metal was too much, the corrosion resistance of the second brazing filler metal was unacceptable.

In Comparative Example 37, since the Cu content of the brazing filler metal was too much, the corrosion resistance of the second brazing filler metal was unacceptable.

In Comparative Examples 46 and 47, the numbers of passes each with a rolling reduction of 30% or more were more than five while the temperatures of the clad materials were 200° C. to 400° C. during the clad hot rolling. Thus, the ratios R1/R2 of the core material crystal grains were more than 0.30 before the brazing, and the formability was unacceptable.

In Comparative Example 48, the temperature at the start of the clad hot rolling was higher than 520° C. Thus, the crystal grain size of the intermediate layer material was less than 60 μm before the brazing, and the crystal grain size of the intermediate layer material was less than 100 μm after the brazing. Therefore, the corrosion resistance of the first brazing filler metal was unacceptable.

In Comparative Example 49, the temperature of the process annealing was lower than 200° C. Thus, the intermediate layer material had a fibrous structure before the brazing, and the crystal grain size of the intermediate layer material was less than 100 μm after the brazing. Therefore, the corrosion resistance of the first brazing filler metal was unacceptable.

In Comparative Example 50, since the temperature of the process annealing was higher than 560° C., the first brazing filler metal melted, and a brazing sheet could not be produced. Thus, the manufacturability was unacceptable.

In Comparative Example 51, the process annealing time was shorter than one hour. Thus, the intermediate layer material had a fibrous structure before the brazing, and the crystal grain size of the intermediate layer material was less than 100 μm after the brazing. Therefore, the corrosion resistance of the first brazing filler metal was unacceptable.

In Comparative Example 52, the heating temperature for the intermediate layer material and the first brazing filler metal was too low, and the start temperature of the hot clad rolling was lower than 400° C. (annealing process was not included). Thus, a crack was caused during the hot clad rolling, and a brazing sheet with the desired thickness could not be produced.

In Comparative Example 53, the heating time for the intermediate layer material and the first brazing filler metal was too short, and the start temperature of the hot clad rolling was lower than 400° C. (annealing process was not included). Thus, a crack was caused during the hot clad rolling, and a brazing sheet with the desired thickness could not be produced.

In Comparative Example 54, since the heating temperature for the intermediate layer material and the first brazing filler metal was too high, the brazing filler metal melted, and a brazing sheet with the desired thickness could not be produced.

INDUSTRIAL APPLICABILITY

The aluminum-alloy clad material according to the invention has high strength after brazing and is excellent in the brazing properties such as the fin joint ratio and the erosion resistance and the corrosion resistance. Thus, the aluminum-alloy clad material is preferably used as a part forming a flow path of an automobile heat exchanger in particular.

REFERENCE SIGNS LIST

R1: Crystal Grain Size in the plate thickness direction in a core material cross section along the rolling direction

R2: Crystal Grain Size in the rolling direction in a core material cross section along the rolling direction 

1. An aluminum-alloy clad material having an aluminum alloy core material, an intermediate layer material clad on one surface of the core material and a brazing filler metal clad on a surface of the intermediate layer material that is not on the core material side, wherein the core material comprises an aluminum alloy comprising 0.05 to 1.50 mass % Si, 0.05 to 2.00 mass % Fe, 0.5 to 2.0 mass % Mn and a balance of Al and unavoidable impurities, the intermediate layer material comprises an aluminum alloy comprises 0.5 to 8.0 mass % Zn, 0.05 to 1.50 mass % Si, 0.05 to 2.00 mass % Fe and a balance of Al and unavoidable impurities, and the brazing filler metal comprises an aluminum alloy comprises 2.5 to 13.0 mass % Si, 0.05 to 1.20 mass % Fe and a balance of Al and unavoidable impurities, a crystal grain size of the intermediate layer material before brazing heating is 60 μm or more, and in a cross section of the core material in a rolling direction before brazing heating, R1/R2 is 0.30 or less, where R1 (μm) is the crystal grain size in a plate thickness direction, and R2 (μm) is the crystal grain size in the rolling direction.
 2. The aluminum-alloy clad material according to claim 1, wherein the core material comprises the aluminum alloy further comprising one or, two or more selected from 0.05 to 0.50 mass % Mg, 0.05 to 1.50 mass % Cu, 0.05 to 0.30 mass % Ti, 0.05 to 0.30 mass % Zr, 0.05 to 0.30 mass % Cr and 0.05 to 0.30 mass % V.
 3. The aluminum-alloy clad material according to claim 1, wherein the intermediate layer material comprises the aluminum alloy further comprising one or, two or more selected from 0.05 to 2.00 mass % Ni, 0.05 to 2.00 mass % Mn, 0.05 to 0.30 mass % Ti, 0.05 to 0.30 mass % Zr, 0.05 to 0.30 mass % Cr and 0.05 to 0.30 mass % V.
 4. The aluminum-alloy clad material according to claim 1, wherein the brazing filler metal comprises the aluminum alloy further comprising one or, two or more selected from 0.5 to 8.0 mass % Zn, 0.05 to 1.50 mass % Cu, 0.05 to 2.00 mass % Mn, 0.05 to 0.30 mass % Ti, 0.05 to 0.30 mass % Zr, 0.05 to 0.30 mass % Cr and 0.05 to 0.30 mass % V.
 5. The aluminum-alloy clad material according to claim 1, wherein the brazing filler metal comprises the aluminum alloy further comprising one or two selected from 0.001 to 0.050 mass % Na and 0.001 to 0.050 mass % Sr.
 6. A method for producing the aluminum-alloy clad material according to claim 1, comprising: a step of casting the aluminum alloys for the core material, the intermediate layer material and the brazing filler metal, respectively, a hot rolling step of hot rolling the cast intermediate layer material ingot and the cast brazing filler metal ingot to predetermined thicknesses, respectively, a cladding step of cladding the intermediate layer material rolled to the predetermined thickness on one surface of the core material ingot, and cladding the brazing filler metal rolled to the predetermined thickness on the surface of the intermediate layer material that is not on the core material side and thus obtaining a clad material, a hot clad rolling step of hot rolling the clad material, a cold rolling step of cold rolling the hot-clad-rolled clad material, and one or more annealing steps of annealing the clad material either during or after the cold rolling step or both during and after the cold rolling step, wherein in the hot clad rolling step, the rolling start temperature is 400 to 520° C., and the number of rolling passes each with a rolling reduction of 30% or more is restricted to five or less while the temperature of the clad material is 200 to 400° C., and the clad material is held at 200 to 560° C. for 1 to 10 hours in the annealing steps.
 7. An aluminum-alloy clad material having an aluminum alloy core material, an intermediate layer material clad on one surface of the core material, a brazing filler metal clad on the surface of the intermediate layer material that is not on the core material side, and a brazing filler metal clad on the other surface of the core material, wherein the core material comprises an aluminum alloy comprising 0.05 to 1.50 mass % Si, 0.05 to 2.00 mass % Fe, 0.5 to 2.0 mass % Mn and a balance of Al and unavoidable impurities, the intermediate layer material comprises an aluminum alloy comprising 0.5 to 8.0 mass % Zn, 0.05 to 1.50 mass % Si, 0.05 to 2.00 mass % Fe and a balance of Al and unavoidable impurities, and the brazing filler metal clad on the surface of the intermediate layer material that is not on the core material side and the brazing filler metal clad on the other surface of the core material comprise an aluminum alloy comprising 2.5 to 13.0 mass % Si, 0.05 to 1.20 mass % Fe and a balance of Al and unavoidable impurities, a crystal grain size of the intermediate layer material before brazing heating is 60 μm or more, and in a cross section of the core material in a rolling direction before brazing heating, R1/R2 is 0.30 or less, wherein R1 (μm) is the crystal grain size in a plate thickness direction, and R2 (μm) is the crystal grain size in the rolling direction.
 8. The aluminum-alloy clad material according to claim 7, wherein the core material comprises the aluminum alloy further comprising one or, two or more selected from 0.05 to 0.50 mass % Mg, 0.05 to 1.50 mass % Cu, 0.05 to 0.30 mass % Ti, 0.05 to 0.30 mass % Zr, 0.05 to 0.30 mass % Cr and 0.05 to 0.30 mass % V.
 9. The aluminum-alloy clad material according to claim 7, wherein the intermediate layer material comprises the aluminum alloy further comprising one or, two or more selected from 0.05 to 2.00 mass % Ni, 0.05 to 2.00 mass % Mn, 0.05 to 0.30 mass % Ti, 0.05 to 0.30 mass % Zr, 0.05 to 0.30 mass % Cr and 0.05 to 0.30 mass % V.
 10. The aluminum-alloy clad material according to claim 7, wherein the brazing filler metal clad on the surface of the intermediate layer material that is not on the core material side and the brazing filler metal clad on the other surface of the core material comprises the aluminum alloy further comprising one or, two or more selected from 0.5 to 8.0 mass % Zn, 0.05 to 1.50 mass % Cu, 0.05 to 2.00 mass % Mn, 0.05 to 0.30 mass % Ti, 0.05 to 0.30 mass % Zr, 0.05 to 0.30 mass % Cr and 0.05 to 0.30 mass % V.
 11. The aluminum-alloy clad material according to claim 7, wherein the brazing filler metal clad on the surface of the intermediate layer material that is not on the core material side and the brazing filler metal clad on the other surface of the core material comprise the aluminum alloy further comprising one or two selected from 0.001 to 0.050 mass % Na and 0.001 to 0.050 mass % Sr.
 12. A method for producing the aluminum-alloy clad material according to claim 7, comprising: a step of casting the aluminum alloys for the core material, the intermediate layer material, the brazing filler metal clad on the surface of the intermediate layer material that is not on the core material side and the brazing filler metal clad on the other surface of the core material, respectively, a hot rolling step of hot rolling the cast intermediate layer material ingot, the cast brazing filler metal ingot clad on the surface of the intermediate layer material that is not on the core material side and the cast brazing filler metal ingot clad on the other surface of the core material to predetermined thicknesses, respectively, a cladding step of cladding the intermediate layer material rolled to the predetermined thickness on one surface of the core material ingot, cladding the brazing filler metal rolled to the predetermined thickness on the surface of the intermediate layer material that is not on the core material side, and cladding the brazing filler metal rolled to the predetermined thickness on the other surface of the core material ingot and thus obtaining a clad material, a hot clad rolling step of hot rolling the clad material, a cold rolling step of cold rolling the hot-clad-rolled clad material, and one or more annealing steps of annealing the clad material either during or after the cold rolling step or both during and after the cold rolling step, wherein in the hot clad rolling step, the rolling start temperature is 400 to 520° C., and the number of rolling passes each with a rolling reduction of 30% or more is restricted to five or less while the temperature of the clad material is 200 to 400° C., and the clad material is held at 200 to 560° C. for 1 to 10 hours in the annealing steps.
 13. A heat exchanger using the aluminum-alloy clad material according to claim 1, wherein the crystal grain size of the intermediate layer material after brazing heating is 100 μm or more.
 14. A method for producing the heat exchanger according to claim 13, wherein an aluminum alloy material is brazed in an inert gas atmosphere with flux.
 15. A heat exchanger using the aluminum-alloy clad material according to claim 7, wherein the crystal grain size of the intermediate layer material after brazing heating is 100 μm or more.
 16. A method for producing the heat exchanger according to claim 15, wherein an aluminum alloy material is brazed in an inert gas atmosphere with flux. 